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Molecular Landscape of Acute Myeloid Leukemia in Pediatric Patient-Age-Related Correlations: A Systematic Review
Katarzyna Cencelewicz1, Barbara Pieniążek1, Joanna Chajec1
1Student Scientific Society of Independent Laboratory of Genetic Diagnostics, Medical University of Lublin, 20-093 Lublin, Poland.
Abstract:
Acute myeloid leukemia (AML) accounts for 15-20% of childhood leukemia cases; however, it is characterized by very high aggressiveness and has the highest mortality rate among leukemias, with relapse rates ranging from 34% to 38%. It is a disease characterized by high molecular diversity, and the frequency of specific genetic alterations in children is different from that in adults. Furthermore, mutations and rearrangements vary with age within the pediatric population. To date, a wide spectrum of genetic alterations has already been studied, but the molecular landscape of each patient is unique. An analysis of rearrangements and mutations specific to children of different ages appears to be crucial in order to individualize diagnosis and therapy appropriately. The aim of the following review is to analyze the molecular landscape of pediatric AML by age in detail in order to prioritize therapeutic strategies dedicated to specific age groups.
Insights
Pediatric acute myeloid leukemia (AML) has high relapse rates and molecular diversity. Analyzing age-specific genetic alterations is crucial for tailoring treatments and improving outcomes in childhood AML.
Area of Science:
- Pediatric Oncology
- Hematology
- Molecular Biology
Background:
- Acute myeloid leukemia (AML) represents 15-20% of childhood leukemia cases.
- AML in children has high aggressiveness, mortality, and relapse rates (34-38%).
- Significant molecular diversity exists, with age-dependent genetic alterations in pediatric AML.
Purpose of the Study:
- To analyze the molecular landscape of pediatric AML stratified by age.
- To identify age-specific genetic alterations for personalized diagnosis and therapy.
- To prioritize therapeutic strategies based on distinct pediatric age groups.
Main Methods:
- Comprehensive review of existing literature on pediatric AML genetics.
- Analysis of reported mutations and rearrangements in different pediatric age cohorts.
- Correlation of molecular findings with clinical outcomes and age-specific patterns.
Main Results:
- Pediatric AML exhibits unique genetic alterations that differ from adult AML.
- Genetic mutations and rearrangements vary significantly across different pediatric age groups.
- Understanding these age-specific molecular profiles is key to individualized treatment.
Conclusions:
- Age-specific molecular analysis is essential for effective pediatric AML management.
- Tailoring therapies based on molecular landscape and age can improve patient outcomes.
- Further research into age-stratified genetic drivers is needed to optimize treatment strategies.
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